Cargando…

Acromegaly remission, SIADH and pituitary function recovery after macroadenoma apoplexy

Pituitary apoplexy is a rare but potentially life-threatening clinical syndrome characterised by ischaemic infarction or haemorrhage into a pituitary tumour that can lead to spontaneous remission of hormonal hypersecretion. We report the case of a 50-year-old man who attended the emergency departmen...

Descripción completa

Detalles Bibliográficos
Autores principales:	Sanz-Sapera, E, Sarria-Estrada, S, Arikan, F, Biagetti, B
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Bioscientifica Ltd 2019
Materias:	Unique/Unexpected Symptoms or Presentations of a Disease
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115412/ https://www.ncbi.nlm.nih.gov/pubmed/31310082 http://dx.doi.org/10.1530/EDM-19-0057

Ejemplares similares

Stubborn hiccups as a sign of massive apoplexy in a naive acromegaly patient with pituitary macroadenoma
por: Simsek Bagir, Gulay, et al.
Publicado: (2017)

Thyrotoxicosis with absence of clinical features of acromegaly in a TSH- and GH-secreting, invasive pituitary macroadenoma
por: Johnston, Philip C, et al.
Publicado: (2015)

A case of pituitary apoplexy in pregnancy
por: Hayes, Aimee R, et al.
Publicado: (2014)

Dense calcification in a GH-secreting pituitary macroadenoma
por: Ibrahim, Ramez, et al.
Publicado: (2014)

An intrasellar pituitary adenoma–gangliocytoma presenting as acromegaly
por: Lee, Melissa H, et al.
Publicado: (2017)

Emergence of a latent TSHoma pituitary macroadenoma on a background of primary autoimmune hypothyroidism
por: Yap, Yew Wen, et al.
Publicado: (2018)

Recurrent pituitary apoplexy due to two successive neoplasms presenting with ocular paresis and epistaxis
por: Teasdale, Stephanie, et al.
Publicado: (2015)

Aneurysmal subarachnoid haemorrhage in the pituitary fossa of a patient with acromegaly – a rare phenomenon
por: Fookeerah, Prishila, et al.
Publicado: (2023)

Acromegaly with empty sella syndrome
por: Daya, Reyna, et al.
Publicado: (2021)

Phaeochromocytoma and Acromegaly: a unifying diagnosis
por: Mumby, C, et al.
Publicado: (2014)

Late presentation of acromegaly in medically controlled prolactinoma patients
por: Manuylova, Ekaterina, et al.
Publicado: (2016)

An unusual case of an ACTH-secreting macroadenoma with a germline variant in the aryl hydrocarbon receptor-interacting protein (AIP) gene
por: Dinesen, Pia T, et al.
Publicado: (2015)

Status epilepticus and diabetes ketoacidosis: uncommon clinical presentations of acromegaly
por: Chamba, Nyasatu G, et al.
Publicado: (2021)

A rare challenging case of co-existent craniopharyngioma, acromegaly and squamous cell lung cancer
por: Fountas, Athanasios, et al.
Publicado: (2018)

Rare association of acromegaly with left atrial myxoma in Carney's complex due to novel PRKAR1A mutation
por: Birla, Shweta, et al.
Publicado: (2014)

Synchronous GH- and prolactin-secreting pituitary adenomas
por: Rahman, Maryam, et al.
Publicado: (2014)

Pituitary metastasis unveiling a lung adenocarcinoma
por: Lopes, Ana M, et al.
Publicado: (2021)

Bacterial meningitis as a first presentation of pituitary macroprolactinoma
por: Margari, Niki, et al.
Publicado: (2014)

Pituitary hyperplasia: an uncommon presentation of a common disease
por: Neves, C P, et al.
Publicado: (2015)

Sellar plasmacytoma presenting with symptoms of anterior pituitary dysfunction
por: Ferreira, Ana G, et al.
Publicado: (2017)

Recurrent pituitary abscess: case report and review of the literature
por: Furnica, Raluca Maria, et al.
Publicado: (2018)

Pituitary abscess: a case report and review of the literature
por: Karagiannis, Apostolos K A, et al.
Publicado: (2016)

Infundibulo-hypophysitis-like radiological image in a patient with pituitary infiltration of a diffuse large B-cell non-Hodgkin lymphoma
por: León-Suárez, A, et al.
Publicado: (2016)

Tuberculosis in the pituitary fossa: a common pathology in an uncommon site
por: Majumdar, K, et al.
Publicado: (2014)

Corticotroph adenoma and pituitary fungal infection: a rare association
por: Catarino, Diana, et al.
Publicado: (2020)

Diabetes insipidus secondary to nivolumab-induced neurohypophysitis and pituitary metastasis
por: Fosci, Michele, et al.
Publicado: (2021)

An FSH and TSH pituitary adenoma, presenting with precocious puberty and central hyperthyroidism
por: Vargas, Guadalupe, et al.
Publicado: (2017)

Thyroid carcinoma with atypical metastasis to the pituitary gland and unexpected postmortal diagnosis
por: Popławska-Kita, Anna, et al.
Publicado: (2020)

Abnormal thyroid function: an unusual presentation of pituitary stalk interruption syndrome
por: Steen, Erica A, et al.
Publicado: (2023)

Two cases of spontaneous remission of primary hyperparathyroidism due to auto-infarction: different management and their outcomes
por: Novodvorsky, Peter, et al.
Publicado: (2019)

Pituitary hyperplasia: case series and literature review of an under-recognised and heterogeneous condition
por: De Sousa, Sunita M C, et al.
Publicado: (2015)

A case of Kallmann syndrome associated with a non-functional pituitary microadenoma
por: Ach, Taieb, et al.
Publicado: (2018)

Silent Crooke’s cell corticotroph adenoma of the pituitary gland presenting as delayed puberty
por: Giri, Dinesh, et al.
Publicado: (2017)

Clinical course of pituitary function and image in IgG4-related hypophysitis
por: Anno, Takatoshi, et al.
Publicado: (2017)

A very rare case of pituitary metastasis infiltrating a non-secretory gonadotroph adenoma
por: Darrat, Milad, et al.
Publicado: (2020)

Ectopic Cushing’s syndrome from an ACTH-producing pheochromocytoma with a non-functioning pituitary adenoma
por: Kishlyansky, David, et al.
Publicado: (2022)

Adult-onset Langerhans cell histiocytosis changing CNS lesion from pituitary to suprasellar extension
por: Kadowaki, Yuji, et al.
Publicado: (2022)

A case of a co-secreting TSH and growth hormone pituitary adenoma presenting with a thyroid nodule
por: Adams, Laura Hamilton, et al.
Publicado: (2018)

Corticotroph pituitary carcinoma with skeletal metastases masquerading as ectopic ACTH syndrome: a long and winding road to diagnosis
por: Van Mieghem, Eugénie, et al.
Publicado: (2022)

A rare case of 46,XX gonadal dysgenesis, Mayer–Rokitansky–Kuster–Hauser syndrome, pituitary and thyroid hypoplasia
por: Ambachew, Rediet, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_d4pbiihlvltqacb4r2qg21l0aq